在资源有限的情况下,心力衰竭患者以用户为中心的慢性护理模式的发展:一项共同设计研究。

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Apinya Koontalay, Mari Botti, Anastasia Hutchinson
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引用次数: 0

摘要

背景:泰国的卫生服务领导者在满足日益增长的中重度慢性心力衰竭(CHF)患者的需求方面面临着重大挑战,这些患者需要在社区进行急性护理管理和持续的支持性护理。大量需要再入院接受高级别护理的CHF患者给卫生保健服务带来了沉重负担。方法:由斯坦福大学Hasso-Plattner设计研究所提出的设计思维模型为开发一种共同设计的、量身定制的、文化上可接受的慢性心力衰竭患者慢性护理模型提供了基础。一名消费者、16名临床医生和两名组织领导人参加了一个包括三个活动的共同设计研讨会。每个活动的目的是(i)定义问题,(ii)头脑风暴可能的解决方案,(iii)开发一个原型解决方案。协同设计研讨会是一个四阶段协同设计项目的一个阶段。收集的数据包括物理数据,如便利贴、故事板和共同设计小组讨论的音频记录。采用内容分析法对数据进行分析。结果:从研讨会活动中产生了9个原型故事板,旨在提高对CHF患者的护理的连续性。拟议的解决方案侧重于改善消费者获得循证信息、多学科专业知识和持续的社区支持的途径。在最终决定最佳模型之前,参与者讨论并评估了每个原型的可行性和可行性。首选的模式是由多学科团队支持的护士领导的病例管理服务。结论:主要利益相关者认识到从短期护理模式转向综合多学科方法以在社区提供长期支持的重要性。最终商定的CHF护士病例管理服务原型由一个多学科团队支持,以社区外展为重点,解决了参与者的主要关切,并被认为是为泰国曼谷城市社区开发CHF慢性护理服务的可行方法。患者或公众贡献:在整个研究过程中,共同设计过程涉及到CHF患者、临床医生和组织领导者的参与和参与。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a User-Centred Chronic Care Model for Patients With Heart Failure in a Limited-Resource Setting: A Codesign Study

Background

Health service leaders in Thailand face substantial challenges in addressing the needs of a growing population of patients with moderate to severe Chronic Heart Failure (CHF) who require acute care management and ongoing supportive care in the community. The large number of CHF patients requiring readmission for high-level care places a significant burden on healthcare services.

Methods

The design thinking model proposed by the Hasso-Plattner Institute of Design at Stanford University underpinned an approach to developing a co-designed, tailored, culturally acceptable model of chronic care for people with CHF. One consumer, 16 clinicians, and two organisational leaders participated in a codesign workshop that included three activities. The purpose of each activity was to (i) define the problem, (ii) brainstorm possible solutions and (iii) develop a prototype solution. The codesign workshop was one phase of a four-phase codesign project. Data collected included physical data such as sticky notes and storyboards and audio recordings of codesign group discussions. Data were analyses using content analysis.

Results

Nine prototype storyboards aimed at enhancing continuity of care for CHF patients emerged from the workshop activities. The proposed solutions focused on improving consumer access to evidence-based information, multidisciplinary expertise and ongoing community support. Participants discussed and evaluated the viability and feasibility of each prototype before reaching a final decision on an optimal model. The preferred model was a nurse-led case management service supported by a multidisciplinary team.

Conclusion

Key stakeholders identified the importance of moving from a short-term model of care to an integrated, multidisciplinary approach to providing long-term support in the community. The final agreed prototype of a CHF Nurse Case Management service supported by a multidisciplinary team with a focus on community outreach addressed the key concerns of participants and was considered a feasible approach to developing a CHF chronic care service for the community in urban Bangkok, Thailand.

Patient or Public Contribution

The process of codesign involved the engagement and participation of individuals with CHF, clinicians and organisational leaders throughout the research process.

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来源期刊
Health Expectations
Health Expectations 医学-公共卫生、环境卫生与职业卫生
CiteScore
5.20
自引率
9.40%
发文量
251
审稿时长
>12 weeks
期刊介绍: Health Expectations promotes critical thinking and informed debate about all aspects of patient and public involvement and engagement (PPIE) in health and social care, health policy and health services research including: • Person-centred care and quality improvement • Patients'' participation in decisions about disease prevention and management • Public perceptions of health services • Citizen involvement in health care policy making and priority-setting • Methods for monitoring and evaluating participation • Empowerment and consumerism • Patients'' role in safety and quality • Patient and public role in health services research • Co-production (researchers working with patients and the public) of research, health care and policy Health Expectations is a quarterly, peer-reviewed journal publishing original research, review articles and critical commentaries. It includes papers which clarify concepts, develop theories, and critically analyse and evaluate specific policies and practices. The Journal provides an inter-disciplinary and international forum in which researchers (including PPIE researchers) from a range of backgrounds and expertise can present their work to other researchers, policy-makers, health care professionals, managers, patients and consumer advocates.
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